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血管性血友病因子,血流中的绝地武士。

von Willebrand factor, Jedi knight of the bloodstream.

作者信息

Springer Timothy A

机构信息

Program in Cellular and Molecular Medicine and Division of Hematology, Department of Medicine, Boston Children's Hospital, and Department of Biological Chemistry and Pharmacology, Harvard Medical School, Boston, MA.

出版信息

Blood. 2014 Aug 28;124(9):1412-25. doi: 10.1182/blood-2014-05-378638. Epub 2014 Jun 13.

Abstract

When blood vessels are cut, the forces in the bloodstream increase and change character. The dark side of these forces causes hemorrhage and death. However, von Willebrand factor (VWF), with help from our circulatory system and platelets, harnesses the same forces to form a hemostatic plug. Force and VWF function are so closely intertwined that, like members of the Jedi Order in the movie Star Wars who learn to use "the Force" to do good, VWF may be considered the Jedi knight of the bloodstream. The long length of VWF enables responsiveness to flow. The shape of VWF is predicted to alter from irregularly coiled to extended thread-like in the transition from shear to elongational flow at sites of hemostasis and thrombosis. Elongational force propagated through the length of VWF in its thread-like shape exposes its monomers for multimeric binding to platelets and subendothelium and likely also increases affinity of the A1 domain for platelets. Specialized domains concatenate and compact VWF during biosynthesis. A2 domain unfolding by hydrodynamic force enables postsecretion regulation of VWF length. Mutations in VWF in von Willebrand disease contribute to and are illuminated by VWF biology. I attempt to integrate classic studies on the physiology of hemostatic plug formation into modern molecular understanding, and point out what remains to be learned.

摘要

血管被割破时,血流中的力会增加并改变性质。这些力的负面影响会导致出血和死亡。然而,在我们的循环系统和血小板的帮助下,血管性血友病因子(VWF)利用同样的力形成止血栓。力与VWF的功能紧密相连,就像电影《星球大战》中学会运用“原力”行善的绝地武士团成员一样,VWF可被视为血流中的绝地骑士。VWF的长链使其能够对血流做出反应。预计在止血和血栓形成部位,从剪切流转变为拉伸流时,VWF的形状会从不规则盘绕变为伸展的丝状。通过其丝状形状的VWF长度传播的拉伸力会暴露其单体,以便与血小板和内皮下层进行多聚体结合,并且可能还会增加A1结构域对血小板的亲和力。在生物合成过程中,特殊结构域将VWF连接并压缩在一起。水动力使A2结构域展开,从而实现VWF长度的分泌后调节。血管性血友病中VWF的突变有助于VWF生物学研究,同时也从VWF生物学研究中得到阐释。我试图将关于止血栓形成生理学的经典研究与现代分子理解相结合,并指出仍有待了解的内容。

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